Probing the kinetic performance limits for ion chromatography. I. Isocratic conditions for small ions

被引:8
作者
Causon, Tim J. [1 ]
Hilder, Emily F. [1 ]
Shellie, Robert A. [1 ]
Haddad, Paul R. [1 ]
机构
[1] Univ Tasmania, Sch Chem, ACROSS, Hobart, Tas 7050, Australia
基金
澳大利亚研究理事会;
关键词
Ion-exchange; Ion chromatography; Kinetic performance; Isocratic; TEMPERATURE LIQUID-CHROMATOGRAPHY; PLOT METHOD; REPRESENTATION; SEPARATIONS; SELECTIVITY; RETENTION; PRESSURES; COLUMNS; ANIONS; SPEED;
D O I
10.1016/j.chroma.2010.05.066
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The first use of the kinetic plot method to characterise the performance of ion-exchange columns for separations of small inorganic anions is reported. The influence of analyte type (mono- and divalent), particle size (5 and 9 mu m), temperature (30 and 60 degrees C) and maximum pressure drop upon theoretical extrapolations was investigated using data collected from anion-exchange polymeric particulate columns. The quality of extrapolations was found to depend upon the choice of analyte, but could be verified by coupling a series of columns to demonstrate some practical solutions for ion chromatography separations requiring relatively high efficiency. Separations of small anions yielding 25-40,000 theoretical plates using five serially connected columns (9 mu m particles) were obtained and yielded deviations of <15% from the kinetic plot predictions. While this approach for achieving high efficiencies results in a very long analysis time (t(0) = 21 min), separations yielding approximately 10,000 theoretical plates using two serially connected columns (t(0) <5 min) were shown to be more practically useful for isocratic separations when compared to use of a single column operated at optimum linear velocity (t(0) > 10 min). (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:5057 / 5062
页数:6
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